WO2009143611A1 - Suppression de production de cytokines pro-inflammatoires pendant une thérapie par réovirus oncolytique - Google Patents

Suppression de production de cytokines pro-inflammatoires pendant une thérapie par réovirus oncolytique Download PDF

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WO2009143611A1
WO2009143611A1 PCT/CA2009/000721 CA2009000721W WO2009143611A1 WO 2009143611 A1 WO2009143611 A1 WO 2009143611A1 CA 2009000721 W CA2009000721 W CA 2009000721W WO 2009143611 A1 WO2009143611 A1 WO 2009143611A1
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reovirus
administered
subject
agent
pro
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PCT/CA2009/000721
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English (en)
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Matthew C. Coffey
Bradley G. Thompson
Hardev Pandha
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Oncolytics Biotech Inc.
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Priority to CN2009801193973A priority Critical patent/CN102065873A/zh
Priority to CA2723587A priority patent/CA2723587C/fr
Priority to AU2009253683A priority patent/AU2009253683B2/en
Priority to JP2011510788A priority patent/JP2011520994A/ja
Priority to EP09753372A priority patent/EP2296679A4/fr
Priority to US12/994,114 priority patent/US8470312B2/en
Priority to MX2010012857A priority patent/MX2010012857A/es
Publication of WO2009143611A1 publication Critical patent/WO2009143611A1/fr
Priority to IL208380A priority patent/IL208380A/en
Priority to ZA2010/08017A priority patent/ZA201008017B/en
Priority to US13/898,771 priority patent/US20130243732A1/en

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66—Microorganisms or materials therefrom
    • A61K35/76—Viruses; Subviral particles; Bacteriophages
    • A61K35/765—Reovirus; Rotavirus
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/28—Compounds containing heavy metals
    • A61K31/282—Platinum compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/555—Heterocyclic compounds containing heavy metals, e.g. hemin, hematin, melarsoprol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00—Medicinal preparations containing inorganic active ingredients
    • A61K33/24—Heavy metals; Compounds thereof
    • A61K33/243—Platinum; Compounds thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2720/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsRNA viruses
    • C12N2720/00011—Details
    • C12N2720/12011—Reoviridae
    • C12N2720/12032—Use of virus as therapeutic agent, other than vaccine, e.g. as cytolytic agent

Definitions

  • BACKGROUND Reovirus is a dsRNA virus with tropism to cancer cells having an activated Ras pathway. It has been demonstrated that administration of reovirus into tumor bearing animals results in generation of a robust anti-viral response mediated by both the humoral and cellular arms of the immune system. This anti-viral response can antagonize the oncolytic effectiveness of the therapeutic virus. As such, combinational use of immune suppressing agents to overcome this immune antagonism of reovirus oncolysis has been explored. It has been demonstrated that co-administration of agents that ablate the generation of neutralizing anti-reovirus antibodies (NARA) can result in morbidity in the test animals.
  • NARA neutralizing anti-reovirus antibodies
  • kits for treating a proliferative disorder in a subject comprising administering to the subject one or more reoviruses and one or more agents that modulate expression or activity of pro-inflammatory cytokines.
  • the agents may inhibit expression or activity of pro-inflammatory cytokines.
  • Figures IA, IB, 1C and ID show reduced tumor growth and increased survival following reovirus/cisplatin combination therapy.
  • Tumors were measured on the days indicated and tumor volume expressed as tumor volume relative to volume at commencement of treatment ( Figures IA and IB). Mice were euthanized when tumors exceeded 15mm in any one dimension. Survival is expressed as Kaplan-Myer plots ( Figures 1C and ID).
  • Figure 2 is a graph showing the neutralizing anti-reovirus antibody (NARA) response after no treatment (control) or treatment with reovirus, cisplatin or the combination of reovirus and cisplatin.
  • NARA neutralizing anti-reovirus antibody
  • Figures 3A, 3B, 3C, 3D, 3E, 3F, and 3G are graphs showing pro-inflammatory cytokine response is abrogated by cisplatin.
  • the response of IL-II ( Figure 3A), IL-3 ( Figure 3B), IL-6 ( Figure 3C), IL- 12 ( Figure 3D), IL- 17 ( Figure 3E), MIP-II ( Figure 3F) and RANTES ( Figure 3G) were measured after no treatment (control) or treatment with reovirus, cisplatin or the combination of reovirus and cisplatin.
  • reoviruses use a host cell's Ras pathway machinery to downregulate double-stranded RNA-activated protein kinase (PKR) and thus replication in the cell.
  • PLR protein kinase
  • Reovirus oncolysis can be enhanced in vitro by the use of cytotoxic agents.
  • cytotoxic agents including: IL-II, IL-3, IL-6, IL- 12 p70, IL- 17, MIP-II, and RANTES.
  • Inhibition of pro-inflammatory cytokines by cisplatin prevents T-cell recognition of reovirus infected cells and allows virus replication to ensue without cellular immunity antagonism.
  • cisplatin allows production of protective neutralizing anti-reovirus antibodies (NARA) NARA and its concomitant benefits (e.g., preventing reovirus toxicities in patients).
  • NARA neutralizing anti-reovirus antibodies
  • platinum compounds to selectively block both innate and adaptive T-cell responses, while having no effect on B-cell activity, has not previously been described.
  • a method of treating a proliferative disorder in a subject comprising administering a reovirus to the subject and administering to the subject an agent that modulates pro-inflammatory cytokines.
  • the agent inhibits the expression or activity of the pro-inflammatory cytokines.
  • the term modulate refers to a change (positive or negative) of 10, 20, 30, 40, 50, 60, 70, 80, 90 percent or greater as compared to a control level.
  • control refers to a reference standard from an untreated sample or subject.
  • a control level is the level of expression or activity in a control sample in the absence of a stimulus. The control can be prior to, after recovery, or without the stimulus.
  • the cytokine modulating agent blocks T-cell responses while having little to no effect on B-cell activity.
  • the agent inhibits pro-inflammatory cytokines but does not inhibit or minimally inhibits production of NARA.
  • the agent is a platinum compound. Suitable platinum compounds include, but are not limited to, cisplatin, carboplatin, metaplatin and oxaliplatin.
  • TNF-I antibodies such as infliximab, CDP571, CDP870, and adalimumab
  • recombinant, human soluble p55 TNF receptors such as onercept
  • soluble TNF receptor and Fc fragment fusion proteins such as etanercept
  • pegylated Fab fragments of humanized antibody to TNF such as certolizumab pegol
  • chimeric antibodies to anti-I chain of IL-2 receptor such as basiliximab or daclizumab
  • IL-12p40 antibodies such as ABT-874
  • IL-6 receptor antibodies such as MRA or tocilizumab
  • IFN-K antibodies such as fontolizumab
  • antibodies that inhibit IL-I binding to the IL-I receptor such as AMG108
  • caspase-1 inhibitors that inhibit cytokine-release such as diarylsulphonylurene
  • IL- 15 antibodies such as mepolizumab
  • Other agents include human recombinant lactoferrin, which inhibits cellular release of proinflammatory cytokines and prometastatic cytokines (including IL-6, IL-8, granulocyte macrophage colony-stimulating factor and TNF- ⁇ ).
  • Inhibitors of dendritic cell derived IL- 12 and IL- 18 such as rapamycin and sanglifehrin are also suitable for use in the provided methods.
  • Rapamycin is an immunosuppressant that inhibits T cell mTOR kinase activation
  • Sanglifehrin A is a cyclophilin-binding immunosuppressant that also inhibits IL-2 dependent T cell proliferation.
  • dietary rutin colitis which suppresses the induction of pro-inflammatory cytokines such as IL- l ⁇ , IL-6, and GM-CS.
  • the method further includes selecting a subject with a proliferative disorder, wherein the subject is in need of inhibition of a pro-inflammatory cytokine response.
  • a subject may include a subject with little response to reovirus alone or with a progressive resistance to reovirus therapy.
  • the term proliferative disorder refers to any cellular disorder in which the cells proliferate more rapidly than normal tissue growth.
  • a proliferative disorder includes, but is not limited to, neoplasms, which are also referred to as tumors.
  • a neoplasm can include, but is not limited to, pancreatic cancer, breast cancer, brain cancer (e.g., glioblastoma), lung cancer, prostate cancer, colorectal cancer, thyroid cancer, renal cancer, adrenal cancer, liver cancer, neurofibromatosis 1 , and leukemia.
  • a neoplasm can be a solid neoplasm (e.g., sarcoma or carcinoma) or a cancerous growth affecting the hematopoietic system (e.g., lymphoma or leukemia).
  • Other proliferative disorders include, but are not limited to, neurofibromatosis.
  • the proliferating cells associated with the disorder may have a mutation in which the Ras gene (or an element of the Ras signaling pathway) is activated, either directly (e.g., by an activating mutation in Ras) or indirectly (e.g., by activation of an upstream or downstream element in the Ras pathway).
  • Activation of an upstream element in the Ras pathway includes, for example, transformation with epidermal growth factor receptor (EGFR) or Sos. See, for example, Wiessmuller and Wittinghofer, 1994, Cellular Signaling 6(3):247 -267; and Barbacid, 1987, Ann. Rev. Biochem. 56, 779-827.
  • EGFR epidermal growth factor receptor
  • Activation of a downstream element in the Ras pathway includes, for example, mutation within B- Raf. See, for example, Brose et al., 2002, Cancer Res. 62:6997-7000.
  • a proliferative disorder that results, at least in part, by the activation of ras, an upstream element of ras, or an element in the ras signaling pathway is referred to herein as a ras-mediated proliferative disorder.
  • the reovirus is useful for treating proliferative disorders caused by mutations or dysregulation of PKR. See, for example, Strong et al., 1998, £M5O J 17:3351-62.
  • the provided methods further comprise the step of selecting a subject with a ras-mediated proliferative disorder.
  • the provided methods comprise the step of determining whether the proliferative disorder is a ras-mediated proliferative disorder.
  • Such methods for determining whether a proliferative disorder has a certain phenotype are known. See, for example, U.S. Patent No. 7,306,902, which is incorporated herein by reference in its entirety.
  • reovirus refers to any virus classified in the reovirus genus, whether naturally occurring, modified, or recombinant. Reoviruses are viruses with a double-stranded, segmented RNA genome.
  • the virions measure 60-80 nm in diameter and possess two concentric capsid shells, each of which is icosahedral.
  • the genome consists of double-stranded RNA in 10-12 discrete segments with a total genome size of 16-27 kbp. The individual RNA segments vary in size.
  • Three distinct but related types of reoviruses have been recovered from many species. All three types share a common complement-fixing antigen.
  • the human reovirus includes three serotypes: type 1 (strain Lang or TlL), type 2 (strain Jones, T2J), and type 3 (strain Dearing or strain Abney, T3D).
  • the three serotypes are easily identifiable on the basis of neutralization and hemagglutinin-inhibition assays.
  • a reovirus according to this disclosure can be a type 3 mammalian orthoreovirus.
  • Type 3 mammalian orthoreoviruses include, without limitation, Dearing and Abney strains (T3D or T3A, respectively). See, for example, ATCC Accession Nos. VR-232 and VR-824.
  • the reovirus may be naturally occurring or modified.
  • the reovirus is naturally- occurring when it can be isolated from a source in nature and has not been intentionally modified by humans in the laboratory.
  • the reovirus can be from a field source, that is, from a human who has been infected with the reovirus.
  • the reovirus may also be selected or mutagenized for enhanced oncolytic activity.
  • the reovirus may be modified but still capable of lytically infecting a mammalian cell having an active ras pathway.
  • the reovirus may be chemically or biochemically pretreated (e.g., by treatment with a protease, such as chymotrypsin or trypsin) prior to administration to the proliferating cells. Pretreatment with a protease removes the outer coat or capsid of the virus and may increase the infectivity of the virus.
  • the reovirus may be coated in a liposome or micelle (Chandran and Nibert, J. of Virology 72(l):467-75 1998).
  • the virion may be treated with chymotrypsin in the presence of micelle-forming concentrations of alkyl sulfate detergents to generate a new infectious subviral particle (ISVP).
  • ISVP infectious subviral particle
  • the reovirus may be a recombinant reovirus.
  • the recombinant reovirus can be a reassortant reovirus, which includes genomic segments from two or more genetically distinct reoviruses. Reassortment of reovirus genomic segments may occur following infection of a host organism with at least two genetically distinct reoviruses. Reassortment of viruses can be generated in cell culture, for example, by co- infection of permissive host cells with genetically distinct reoviruses.
  • the provided methods include the use of a recombinant reovirus resulting from reassortment of genome segments from two or more genetically distinct reoviruses, including but not limited to, human reovirus, such as type 1 (e.g., strain Lang), type 2 (e.g., strain Jones), and type 3 (e.g., strain Dearing or strain Abney); non-human mammalian reoviruses; or avian reovirus.
  • Recombinant reovirus can also be made by genetic engineering, chemically synthesized, or treatment with chemical or physical mutagens.
  • the provided methods include the use of recombinant reoviruses resulting from reassortment of genome segments from two or more genetically distinct reoviruses wherein at least one parental virus is genetically engineered, comprises one or more chemically synthesized genomic segment, has been treated with chemical or physical mutagens, or is itself the result of a recombination event.
  • the provided methods include the use of the recombinant reovirus that has undergone recombination in the presence of chemical mutagens, including but not limited to, dimethyl sulfate and ethidium bromide, or physical mutagens, including but not limited to, ultraviolet light and other forms of radiation.
  • the provided methods include the use of reoviruses with mutations (including insertions, substitutions, deletions or duplications) in one or more genome segments.
  • mutations can comprise additional genetic information as a result of recombination with a host cell genome or can comprise synthetic genes.
  • mutant reoviruses as described herein can contain a mutation that reduces or essentially eliminates expression of a sigma3 polypeptide or that results in the absence of a functional sigma3 polypeptide as described in U.S. Serial No. 12/124,522, which is incorporated by reference herein in its entirety.
  • a mutation that eliminates expression of a sigma3 polypeptide or that results in the absence of a functional sigma3 polypeptide can be in the nucleic acid encoding the sigma3 polypeptide (i.e., the S4 gene) or in a nucleic acid that encodes a polypeptide that regulates the expression or function of the sigma3 polypeptide.
  • a mutation that reduces the expression of a sigma3 polypeptide refers to a mutation that results in a decrease in the amount of sigma3 polypeptides, compared to a reovirus expressing wild type levels of sigma3 polypeptide, of at least 30% (e.g., at least 40%, 50%, 60%, 70%, 80%, 90%, or 95%).
  • a mutation that essentially eliminates expression of a sigma3 polypeptide refers to a mutation that results in a decrease in the amount of sigma3 polypeptides, relative to the amount of sigma3 polypeptides produced by a wild type reovirus, of at least 95% (e.g., 96%, 97%, 98%, 99%, or 100%).
  • a mutation that results in a decrease in or absence of a functional sigma3 polypeptide refers to a mutation that allows expression of the sigma3 polypeptide but that results in a sigma3 polypeptide that is not able to assemble or incorporate into the viral capsid. It would be understood that it may be desirable or necessary for sigma3 polypeptides to retain other functionalities (e.g., the ability to bind RNA) in order that the mutant reovirus retain the ability to propagate.
  • a mutation in a sigma3 polypeptide as described herein can result in a sigma3 polypeptide that is incorporated into the capsid at levels that are reduced relative to a sigma3 polypeptide that does not contain the mutation (e.g., a wild type sigma3 polypeptide).
  • a mutation in a sigma3 polypeptide as described herein also can result in a sigma3 polypeptide that cannot be incorporated into a viral capsid.
  • a sigma3 polypeptide may have reduced function or lack function due, for example, to an inability of the sigma3 polypeptide and the mul polypeptide to bind appropriately, or due to a conformational change that reduces or prohibits incorporation of the sigma3 polypeptide into the capsid.
  • a mutant reovirus as described herein also can contain one or more further mutations (e.g., a second, third, or fourth mutation) in one of the other reovirus capsid polypeptides (e.g., mul, Iambda2, and/or sigmal).
  • Reo viruses containing a mutation affecting the sigma3 polypeptide and, optionally, a further mutation in any or all of the other outer capsid proteins can be screened for the ability of such mutant reoviruses to infect and cause lysis of cells.
  • neoplastic cells that are resistant to lysis by wild type reovirus can be used to screen for effective mutant reoviruses described herein.
  • a further mutation can reduce or essentially eliminate expression of a mul polypeptide or result in the absence of a functional mul polypeptide.
  • the mul polypeptide which is encoded by the M2 gene, is likely involved in cell penetration and may play a role in transcriptase activation.
  • Each virion contains about 600 copies of mul polypeptides, which are present in the form of 1 :1 complexes with sigma3 polypeptides.
  • the mul polypeptide is myristolated on its N-terminus, and then the myristolated N- terminal 42 residues are cleaved off, resulting in a C-terminal fragment (mul C).
  • a further mutation can reduce or essentially eliminate expression of a Iambda2 polypeptide or result in the absence of a functional Iambda2 polypeptide, and/or a further mutation can reduce or essentially eliminate expression of a sigmal polypeptide or result in the absence of a functional sigmal polypeptide.
  • the Iambda2 polypeptide is encoded by the L2 gene and is involved in particle assembly, and exhibits guanylyltransferase and methyltransferase activity.
  • the sigmal polypeptide is encoded by the S 1 gene and is involved in cell-attachment and serves as the viral hemagglutinin.
  • the reovirus has a lambda-3 polypeptide having one or more amino acid modifications; a sigma-3 polypeptide having one or more amino acid modifications; a mu-1 polypeptide having one or more amino acid modifications; and/or a mu-2 polypeptide having one or more amino acid modifications, as described in U.S. Serial No. 12/046,095, which is incorporated by reference herein in its entirety.
  • the one or more amino acid modifications in the lambda-3 polypeptide are a VaI at residue 214, an Ala at residue 267, a Thr at residue 557, a Lys at residue 755, a Met at residue 756, a Pro at residue 926, a Pro at residue 963, a Leu at residue 979, an Arg at residue 1045, a VaI at residue 1071, or any combination thereof, numbered relative to GenBank Accession No. M24734.1. It is noted that, when the amino acid sequence is a VaI at residue 214 or a VaI at residue 1071, the amino acid sequence further includes at least one additional change in the amino acid sequence.
  • the lambda-3 polypeptide includes the sequence shown in SEQ ID NO: 18.
  • the one or more amino acid modifications in the sigma-3 polypeptide are a Leu at residue 14, a Lys at residue 198, or any combination thereof, numbered relative to GenBank Accession No. K02739. It is noted that, when the amino acid sequence is a Leu at residue 14, the amino acid sequence further includes at least one additional change in the amino acid sequence.
  • the sigma-3 polypeptide includes the sequence shown in SEQ ID NO: 14. Further by way of example, the one or more amino acid modifications in the mu-1 polypeptide is an Asp at residue 73 numbered relative to GenBank Accession No. M20161.1.
  • the mu-1 polypeptide includes the sequence shown in SEQ ID NO: 16.
  • the amino acid modification mu-2 polypeptide is a Ser at residue 528 numbered relative to GenBank Accession No. AF461684.1.
  • the mu-1 polypeptide includes the sequence shown in SEQ ID NO: 15.
  • a reovirus as described herein having one or more modifications can further include a reovirus sigma-2 polypeptide.
  • Such a sigma-2 polypeptide has a Cys at one or more of position 70, 127, 195, 241, 255, 294, 296, or 340, numbered relative to GenBank Accession No. NP_694684.1.
  • the sigma-2 polypeptide includes the sequence shown in SEQ ID NO: 12.
  • the reovirus has a Ll genome segment having one or more nucleic acid modifications; a S4 genome segment having one or more nucleic acid modifications; a Ml genome segment having one or more nucleic acid modifications; and/or a M2 genome segment having one or more nucleic acid modifications, as described in U.S. Serial No. 12/046,095, which is incorporated by reference herein in its entirety.
  • the one or more nucleic acid modifications in the Ll genome segment are a T at position 660, a G at position 817, an A at position 1687, a G at position 2283, an ATG at positions 2284-2286, a C at position 2794, a C at position 2905, a C at position 2953, an A at position 3153, or a G at position 3231 , numbered relative to GenBank Accession No. M24734.1.
  • the Ll genome segment includes the sequence shown in SEQ ID NO: 8.
  • the one or more nucleic acid modifications in the S4 genome segment is an A at position 74 and an A at position 624, numbered relative to GenBank Accession No. K02739.
  • the S4 genome segment includes the sequence shown in SEQ ID NO:4.
  • the nucleic acid modification in the M2 genome segment can be a C at position 248, numbered relative to GenBank Accession No. M20161.1.
  • the M2 genome segment includes the sequence shown in SEQ ID NO:6.
  • the nucleic acid modification in the Ml genome segment is a T at position 1595, numbered relative to GenBank Accession No. AF461684.1.
  • the Ml genome segment includes the sequence shown in SEQ ID NO:5.
  • a reovirus as described herein can include any modification or combination of modifications disclosed herein.
  • a reovirus as described herein includes genomic segments having the sequences shown in SEQ ID NOs: 1-10 or the polypeptides shown in SEQ ID NOs:ll, 12, and 16-21, and either or both SEQ ID NO: 13 or 14.
  • a reovirus as disclosed herein is identified as IDAC Accession No. 190907-01.
  • a mutation or modification as referred to herein can be a substitution, insertion or deletion of one or more nucleotides.
  • Point mutations include, for example, single nucleotide transitions (purine to purine or pyrimidine to pyrimidine) or transversions (purine to pyrimidine or vice versa) and single- or multiple-nucleotide deletions or insertions.
  • a mutation in a nucleic acid can result in one or more conservative or non- conservative amino acid substitutions in the encoded polypeptide, which may result in conformational changes or loss or partial loss of function, a shift in the reading frame of translation (frame-shift) resulting in an entirely different polypeptide encoded from that point on, a premature stop codon resulting in a truncated polypeptide (truncation), or a mutation in a reovirus nucleic acid may not change the encoded polypeptide at all (silent or nonsense). See, for example, Johnson and Overington, 1993, J. MoI. Biol. 233:716-38; Henikoff and Henikoff, 1992, Proc. Natl. Acad. Sci.
  • Mutations can be generated in the nucleic acid of a reovirus using any number of methods known in the art.
  • site directed mutagenesis can be used to modify a reovirus nucleic acid sequence.
  • One of the most common methods of site-directed mutagenesis is oligonucleotide-directed mutagenesis.
  • oligonucleotide-directed mutagenesis an oligonucleotide encoding the desired change(s) in sequence is annealed to one strand of the DNA of interest and serves as a primer for initiation of DNA synthesis.
  • nucleic acids containing a mutation can be generated using PCR or chemical synthesis, or polypeptides having the desired change in amino acid sequence can be chemically synthesized. See, for example, Bang and Kent, 2005, Proc. Natl. Acad. Sci. USA 102:5014-9 and references therein.
  • nucleic acids from reovirus particles can be isolated using standard commercially available nucleic acid methodology. See also, for example, Schiff et al., "Orthoreoviruses and Their Replication," Ch 52, in Fields Virology, Knipe and Howley, eds., 2006, Lippincott Williams and Wilkins.
  • isolated nucleic acids refer to nucleic acids that are separated from other nucleic acids with which they are usually associated.
  • an isolated nucleic acid includes, without limitation, reoviral nucleic acid that is essentially free of non-reoviral (e.g., host cell) nucleic acid, or a reoviral genomic segment that is essentially free of nucleic acid corresponding to other genomic segments.
  • an isolated nucleic acid can include an engineered nucleic acid such as a recombinant or synthetic nucleic acid.
  • a mutant reovirus as described herein can be generated by reconstituting genome segments containing at least a mutation or modification using methods known in the art. See, for example, Schiff et al., "Orthoreoviruses and Their Replication," Ch 52, in Fields Virology, Knipe and Howley, eds., 2006, Lippincott Williams and Wilkins; Smith et al., 1969, Virology 39(4):791-810; and U.S. Patent Nos. 7,186,542; 7,049,127; 6,808,916; and 6,528,305.
  • a mutant reovirus also can be generated by expressing the reovirus genome segments using a plasmid-based reverse genetic system to produce an ISVP.
  • a genetically-engineered or mutant ISVP is a mutant reovirus and refers to an ISVP generated from a reovirus carrying a genetically-engineered or a spontaneously generated mutation affecting at least the sigma3 polypeptide.
  • the ISVPs described herein are stable and can be propagated as ISVPs for multiple (e.g., more than one, e.g., 2, 3, 4, 5, 10, 20, 50, or more) passages.
  • mutant reoviruses described herein produced via a genetically-engineered ISVP or via a plasmid-based reverse genetic system, can be cultured in, for example, human neoplastic cells or L929 mouse fibroblast cells.
  • Mutant reoviruses disclosed herein can be cultured in cells that are only permissive to reovirus strains lacking the sigma3 polypeptide. Using such cell lines to passage the mutant reoviruses described herein can allow for selection of the mutants and also can be used to reduce or prevent reversions of the mutation(s).
  • the mutant reoviruses described herein optionally, exhibit increased infectivity and/or decreased immunogenicity as compared to a non-mutant reovirus (e.g., a control reovirus) and can be selected on the basis of such traits.
  • Increased infectivity can be evidenced by an increase in the range of neoplastic cells and/or the number of cells that are infected by a mutant reovirus compared to a reovirus that expresses a functional sigma3 polypeptide (e.g., an intact virion; e.g., a wild type reovirus).
  • mutant reoviruses described herein also can be screened and selected for other desirable traits including, but not limited to, a faster rate of replication; a faster rate of packaging; the ability to induce apoptosis; the ability to affect lysis in and effectively kill human neoplastic cells lines; the ability to release effective tumor epitopes; interaction with standard chemotherapies; and an increased number of viral progeny.
  • mutant reoviruses can be selected for the ability to lytically infect a neoplastic cell (e.g., a mammalian cell having an active Ras pathway). See, for example, U.S. Patent No. 7,052,832.
  • the reovirus is optionally a reovirus modified to reduce or eliminate an immune reaction to the reovirus.
  • a modified reovirus is referred to herein as an immunoprotected reovirus.
  • modifications include, but are not limited to, packaging of the reovirus in a liposome, a micelle, or other vehicle to mask the reovirus from the immune system.
  • the outer capsid of the reovirus virion particle may be removed since the proteins present in the outer capsid are the major determinant of the host humoral and cellular responses.
  • Reoviruses can be purified using standard methodology. See, for example, Schiff et al., "Orthoreoviruses and Their Replication," Ch 52, in Fields Virology, Knipe and Howley, eds., 2006, Lippincott Williams and Wilkins; Smith et al., 1969, Virology
  • purified mutant reoviruses refer to reoviruses that have been separated from cellular components that naturally accompany them. Typically, reoviruses are considered purified when they are at least 70% (e.g., at least 75%, 80%, 85%, 90%, 95%, or 99%) by dry weight, free from the proteins and other cellular components with which they are naturally associated.
  • reoviruses and agents can be administered in vitro or in vivo in a pharmaceutically acceptable carrier.
  • pharmaceutical compositions that include a reovirus and/or agent that inhibits pro-inflammatory cytokines as described herein are provided. See, for example, U.S. Patent No. 6,576,234 regarding reoviruses.
  • a pharmaceutical composition typically includes a pharmaceutically acceptable carrier.
  • a pharmaceutically acceptable carrier can be a solid, semi-solid, or liquid material that can act as a vehicle, carrier or medium for the reovirus.
  • compositions containing a reovirus and/or the provided agents can be in the form of tablets, pills, powders, lozenges, sachets, elixirs, suspensions, emulsions, solutions, syrups, aerosols (as a solid or in a liquid medium), ointments containing, for example, up to 10% by weight of the active compound, soft and hard gelatin capsules, suppositories, sterile injectable solutions, and sterile packaged powders.
  • the compositions containing a reovirus are suitable for infusion.
  • intravenous infusions there are two types of fluids that are commonly used, crystalloids and colloids.
  • Crystalloids are aqueous solutions of mineral salts or other water-soluble molecules. Colloids contain larger insoluble molecules, such as gelatin; blood itself is a colloid. The most commonly used crystalloid fluid is normal saline, a solution of sodium chloride at 0.9% concentration, which is close to the concentration in the blood (isotonic). Ringer's lactate or Ringer's acetate is another isotonic solution often used for large- volume fluid replacement. A solution of 5% dextrose in water, sometimes called D5W, is often used instead if the patient is at risk for having low blood sugar or high sodium.
  • suitable carriers include phosphate-buffered saline or another physiologically acceptable buffer, lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, calcium phosphate, alginates, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, sterile water, syrup, and methyl cellulose.
  • a pharmaceutical composition additionally can include, without limitation, lubricating agents such as talc, magnesium stearate, and mineral oil; wetting agents; emulsifying and suspending agents; preserving agents such as methyl- and propylhydroxy-benzoates; sweetening agents; and flavoring agents.
  • compositions can be formulated to provide quick, sustained or delayed release of a mutant reovirus after administration by employing procedures known in the art.
  • suitable formulations for use in a pharmaceutical composition can be found in Remington: The Science and Practice of Pharmacy (21th ed.) ed. David B. Troy, Lippincott Williams & Wilkins, 2005.
  • a mutant reovirus can be mixed with a pharmaceutical carrier to form a solid composition.
  • tablets or pills can be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action.
  • a tablet or pill can comprise an inner dosage and an outer dosage component, the latter being in the form of an envelope over the former.
  • the two components can be separated by an enteric layer which serves to resist disintegration in the stomach and permit the inner component to pass intact into the duodenum or to be delayed in release.
  • enteric layers or coatings such materials including a number of polymeric acids and mixtures of polymeric acids with such materials as shellac, cetyl alcohol, and cellulose acetate.
  • Liquid formulations that include a reovirus and/or other agents for oral administration or for injection generally include aqueous solutions, suitably flavored syrups, aqueous or oil suspensions, and flavored emulsions with edible oils such as corn oil, cottonseed oil, sesame oil, coconut oil, or peanut oil, as well as elixirs and similar pharmaceutical vehicles.
  • compositions for inhalation or insufflation include solutions and suspensions in pharmaceutically acceptable, aqueous or organic solvents, or mixtures thereof, and powders. These liquid or solid compositions may contain suitable pharmaceutically acceptable excipients as described herein. Such compositions can be administered by the oral or nasal respiratory route for local or systemic effect.
  • Compositions in pharmaceutically acceptable solvents may be nebulized by use of inert gases. Nebulized solutions may be inhaled directly from the nebulizing device or the nebulizing device may be attached to a face mask tent or intermittent positive pressure breathing machine. Solution, suspension, or powder compositions may be administered, orally or nasally, from devices which deliver the formulation in an appropriate manner.
  • transdermal delivery devices e.g., patches
  • transdermal patches may be used to provide continuous or discontinuous infusion of a mutant reovirus as described herein.
  • the construction and use of transdermal patches for the delivery of pharmaceutical agents is well known in the art. See, for example, U.S. Patent No. 5,023,252.
  • patches can be constructed for continuous, pulsatile, or on-demand delivery of mutant reoviruses.
  • reoviruses and/or other agents are, if necessary, coated in a liposome or micelle to reduce or prevent an immune response in a mammal that has developed immunity toward a reovirus.
  • compositions are referred to as immunoprotected reoviruses and/or agents. See, for example, U.S. Patent Nos. 6,565,831 and 7,014,847.
  • a mutant reovirus as disclosed herein e.g., one that lacks or is deficient in sigma3 polypeptide or function
  • the reovirus is administered in a manner so that it can ultimately contact the target tumor or tumor cells, for example, systemically.
  • the route by which the reovirus is administered, as well as the formulation, carrier or vehicle, depends on the location as well as the type of the target cells.
  • a wide variety of administration routes can be employed.
  • the reovirus can be administered by injection directly to the tumor.
  • the reovirus can be administered intravenously or intravascularly.
  • the reovirus is administered in a manner such that it can be transported systemically through the body of the mammal and thereby reach the tumor (e.g., intravenously or intramuscularly).
  • the reovirus can be administered directly to a single solid tumor, where it then is carried systemically through the body to metastases.
  • the reovirus can also be administered subcutaneously, intraperitoneally, intrathecally (e.g., for brain tumor), topically (e.g., for melanoma), orally (e.g., for oral or esophageal cancer), rectally (e.g., for colorectal cancer), vaginally (e.g., for cervical or vaginal cancer), nasally, by inhalation spray or by aerosol formulation (e.g., for lung cancer).
  • intrathecally e.g., for brain tumor
  • topically e.g., for melanoma
  • orally e.g., for oral or esophageal cancer
  • rectally e.g., for colorectal cancer
  • vaginally e.g., for cervical or vaginal cancer
  • nasally by inhalation spray or by aerosol formulation (e.g., for lung cancer).
  • the virus is administered continuously to a subject at least once per day or up to throughout the day on consecutive days, for a period of time.
  • the virus is administered, for example, to subjects by means of intravenous administration in any pharmacologically acceptable solution, or as an infusion over a period of time.
  • the substance may be administered systemically by injection (e.g., IM or subcutaneously) or taken orally daily at least once per day, or administered by infusion in a manner that results in the daily delivery into the tissue or blood stream of the subject.
  • the period of time is, for example, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, or 24 hours, or any time between 1 and 24 hours, inclusive, or more.
  • the period of time is 5, 15, 30, 60, 90, 120, 150 or 180 minutes, or any time between 5 and 180 minutes, inclusive, or more.
  • the virus is administered by infusion for 60 minutes or about 60 minutes. Administrations can be repeated daily for 2, 3, 4, 5, 6, 7, 8, 9, 10, 14, 21, 28 days or any number of days between 2 and 28 days, inclusive, or longer.
  • Therapeutic agents such as the agents that inhibit production of pro-inflammatory cytokines, of the provided methods are also administered via a wide variety of administration routes.
  • the agents are administered via any of several routes of administration, including, topically, orally, parenterally, intravenously, intraperitoneally, intramuscularly, subcutaneously, intracavity, transdermally, intrahepatically, intracranially, nebulization/inhalation, or by instillation via bronchoscopy.
  • the therapeutic agents are administered continuously in the manner set forth in the description above with respect to oncolytic viruses.
  • the agent is administered, for example, to subjects by means of intravenous administration in any pharmacologically acceptable solution, or as an infusion over a period of time.
  • the agents are administered locally at or near the site of the tumor.
  • the agents are administered systemically.
  • the agents that inhibit pro-inflammatory cytokines are administered in an amount sufficient (i.e., an effective amount) to inhibit one or more pro- inflammatory cytokines.
  • effective amounts of platinum compounds include from about 5 to 1000 mg/m 2 of tumor volume, or any amount in between 5 and 1000 mg/m 2 , inclusive, or more.
  • effective amounts of cisplatin include from about 175-200 mg/m 2 and effective mounts for carboplatin include from about 100- 600 mg/m 2 .
  • Effective amounts of other agents range from 0.001-10,000 mg/kg body weight or any amount in between 0.001 and 10,000 mg/kg body weight, inclusive.
  • effective amounts of platinum compounds include approximately 2 to 7 mg/niL minute (AUC) as calculated by the Calvert formula.
  • effective amounts of platinum compounds include approximately 5 or 6 mg/mL minute (AUC) as calculated by the Calvert formula.
  • the platinum compounds are administered as an intravenous infusion over a period of 30 minutes.
  • the reovirus is administered in an amount that is sufficient to treat the proliferative disorder (e.g., an effective amount).
  • a proliferative disorder is treated when administration of a reovirus to proliferating cells affects lysis (e.g., oncolysis) of the affected cells, resulting in a reduction in the number of abnormally proliferating cells, a reduction in the size of a neoplasm, and/or a reduction in or elimination of symptoms (e.g., pain) associated with the proliferating disorder.
  • lysis e.g., oncolysis
  • the term oncolysis means at least 10% of the proliferating cells are lysed (e.g., at least about 20%, 30%, 40%, 50%, or 75% of the cells are lysed).
  • the percentage of lysis can be determined, for example, by measuring the reduction in the size of a neoplasm or in the number of proliferating cells in a mammal, or by measuring the amount of lysis of cells in vitro (e.g., from a biopsy of the proliferating cells).
  • An effective amount of a virus will be determined on an individual basis and may be based, at least in part, on the particular virus used; the individual's size, age, gender; and the size and other characteristics of the abnormally, proliferating cells. For example, for treatment of a human, approximately 10 3 to 10 12 plaque forming units (PFU) of a virus are used, depending on the type, size and number of proliferating cells or neoplasms present.
  • PFU plaque forming units
  • the effective amount can be, for example, from about 1.0 PFU/kg body weight to about 10 15 PFU/kg body weight (e.g., from about 10 2 PFU/kg body weight to about 10 13 PFU/kg body weight).
  • the effective amount is about IxIO 8 to about IxIO 12 TCID 50 .
  • the effective amount is about IxIO 10 TCID 50 .
  • the agent that inhibits pro-inflammatory cytokines is administered as a thirty minute to one hour intravenous infusion.
  • the reovirus is administered as a one hour intravenous infusion.
  • Optimal dosages of viruses and therapeutic agents and compositions comprising viruses and agents depend on a variety of factors. The exact amount required will vary from subject to subject, depending on the species, age, weight and general condition of the subject, the severity of the disease being treated, the particular virus or vector used and its mode of administration. Thus, it is not possible to specify an exact amount for every composition. However, an appropriate amount can be determined by one of ordinary skill in the art using only routine experimentation given the guidance provided herein. Effective dosages and schedules for administering the compositions may be determined empirically. For example, animal models for a variety of proliferative disorders can be obtained from The Jackson Laboratory, 600 Main Street, Bar Harbor, Maine 04609 USA.
  • Both direct (e.g., histology of tumors) and functional measurements (e.g., survival of a subject or size of a tumor) can be used to monitor response to therapies. These methods involve the sacrifice of representative animals to evaluate the population, increasing the animal numbers necessary for the experiments. Measurement of luciferase activity in the tumor provides an alternative method to evaluate tumor volume without animal sacrifice and allowing longitudinal population-based analysis of therapy.
  • the dosage ranges for the administration of compositions are those large enough to produce the desired effect in which the symptoms of the disease are affected.
  • the dosage should not be so large as to cause adverse side effects, such as unwanted cross- reactions and anaphylactic reactions.
  • the dosage can be adjusted by the individual physician in the event of any counterindications.
  • Dosages vary and are administered in one or more dose administrations daily, for one or several days.
  • the provided viruses and therapeutic agents are administered in a single dose or in multiple doses (e.g., two, three, four, six, or more doses).
  • the infusion can be a single sustained dose or can be delivered by multiple infusions. Treatment may last from several days to several months or until diminution of the disease is achieved.
  • Combinations of the provided viruses and therapeutic agents are administered either concomitantly (e.g., as an admixture), separately but simultaneously (e.g., via separate intravenous lines into the same subject), or sequentially (e.g., one of the compounds or agents is given first followed by the second).
  • the term combination is used to refer to concomitant, simultaneous, or sequential administration of two or more agents.
  • the agent that inhibits proinflammatory cytokines is administered prior to or at the same time as the oncolytic virus.
  • the first compound is administered minutes, hours, days, or weeks prior to administration of the second compound.
  • the first compound can be administered at 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 24, 36, 48, 60, or 72 hours, or any time between 1 and 72 hours, inclusive, prior to administration of a second compound.
  • the first compound is administered more than 72 hours prior to the second compound.
  • the first compound can be administered at 1, 5, 15, 30, 60, 90, or 120 minutes, or any time between 1 and 120 minutes, inclusive, prior to administration of a second compound.
  • the first compound is administered at 1, 2, 3, 4, 5, 6, 7, 14, 21, or 28 days, or any amount in between 1 and 28, inclusive, days prior to administration of the second compound.
  • the first compound is administered more than 28 days prior to the second compound.
  • the agent that inhibits proinflammatory cytokines is administered from about 1 to 8 hours prior to administration of the oncolytic virus.
  • the agent that inhibits pro-inflammatory cytokines is administered at a time of about one hour prior to administration of the oncolytic virus.
  • one cycle of treatment includes administering the agent that inhibits proinflammatory cytokines and the oncolytic virus includes on day 1. On days 2, 3, 4 and 5, only the oncolytic virus is administered to the subject.
  • the subject receives multiple cycles of treatment, for example, two, three, four, five or more cycles of treatment.
  • kits also includes one or more agents or pharmaceutical compositions comprising such agents that inhibit pro-inflammatory cytokines. It is contemplated that a kit, optionally, also includes one or more chemotherapeutic agents, one or more immunosuppressive agents, and/or one or more anti-antireovirus antibodies.
  • a pharmaceutical composition can be formulated in a unit dosage form.
  • unit dosage forms refers to physically discrete units suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of a mutant reovirus calculated to produce the desired therapeutic effect in association with a suitable pharmaceutically acceptable carrier.
  • the provided methods may be combined with other tumor therapies such as chemotherapy, radiotherapy, surgery, hormone therapy and/or immunotherapy.
  • the oncolytic virus may be administered in conjunction with surgery or removal of the neoplasm. Therefore, provided herewith are methods for the treatment of a solid neoplasm comprising surgical removal of the neoplasm and administration of an oncolytic virus at or near to the site of the neoplasm.
  • the compositions in the provided methods are, optionally, administered in conjunction with or in addition to known anticancer compounds or chemotherapeutic agents.
  • Chemotherapeutic agents are compounds which may inhibit the growth of tumors. Such agents, include, but are not limited to.
  • 5- fluorouracil Mitomycin C, methotrexate, hydroxyurea, cyclophosphamide, dacarbazine, mitoxantrone, anthracyclins (Epirubicin and Doxurubicin), antibodies to receptors, such as herceptin, etopside, pregnasome, hormone therapies such as tamoxifen and anti- estrogens, interferons, aromatase inhibitors, progestational agents and LHRH analogs.
  • hormone therapies such as tamoxifen and anti- estrogens, interferons, aromatase inhibitors, progestational agents and LHRH analogs.
  • treatment refers to a method of reducing the effects of a disease or condition or symptom of the disease or condition.
  • treatment can refer to a 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or 100% reduction or amelioration in the severity of an established disease or condition or symptom of the disease or condition.
  • the method for treating cancer is considered to be a treatment if there is a 10% reduction in one or more symptoms of the disease in a subject as compared to control.
  • the reduction can be a 10, 20, 30, 40, 50, 60, 70, 80, 90, 100% or any percent reduction in between 10 and 100 as compared to native or control levels. It is understood that treatment does not necessarily refer to a cure or complete ablation of the disease, condition or symptoms of the disease or condition.
  • references to decreasing, reducing, or inhibiting include a change of 10, 20, 30, 40, 50 ,60, 70 ,80, 90 percent or greater as compared to a control level. Such terms can include but do not necessarily include complete elimination.
  • the term subject can be a vertebrate, more specifically a mammal (e.g., a human, horse, pig, rabbit, dog, sheep, goat, non-human primate, cow, cat, guinea pig or rodent), a fish, a bird or a reptile or an amphibian.
  • a mammal e.g., a human, horse, pig, rabbit, dog, sheep, goat, non-human primate, cow, cat, guinea pig or rodent
  • a fish e.g., a fish
  • bird or a reptile or an amphibian e.g., a particular age or sex.
  • patient or subject may be used interchangeably and can refer to a subject with a disease or disorder.
  • patient or subject includes human and veterinary subjects.
  • RV Reovirus type 3 Dearing
  • CIV combination index value
  • mice bearing subcutaneous B16.F10 and K1735 tumors respectively were treated on days 1 and 4 with either reovirus alone i.t. (squares), cisplatin alone i.p. (triangles), or reovirus and cisplatin in combination (circles).
  • Control treated mice received PBS. Tumors were measured on the days indicated and tumor volume expressed as tumor volume relative to volume at commencement of treatment ( Figures IA and IB). Mice were euthanized when tumors exceeded 15mm in any one dimension. Survival is expressed as Kaplan-Myer plots ( Figures 1C and ID).
  • mice treated with RV/CP combination therapy compare to single agent treatments ( Figures IA, IB, 1C and ID).
  • Mean relative tumor volumes ⁇ SD at day 12 were, control: all reached endpoint, RV alone: 8.92 ⁇ 6.94, CP alone: 9.87 ⁇ 2.80, RV plus CP: 3.86 ⁇ 2.24.
  • Median survival (days) were, control: 6, RV: 12, CP: 8, combination of RV and CP: 17.
  • Live virus was recovered from the tumors of all RV only treated animals and from the liver and heart of 1/6 mice. In contrast live virus was detected in only 50% of tumors from combination treated mice but in the liver of 4/6 mice.
  • CP did not affect the neutralizing anti-reovirus antibody (NARA) response to RV ( Figure 2), but caused a marked attenuation of production of proinflammatory cytokines to RV when used in combination ( Figures 3A, 3B, 3C, 3D, 3E, 3F, and 3G).
  • NARA neutralizing anti-reovirus antibody

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Abstract

La présente invention concerne des procédés de traitement de troubles prolifératifs chez un sujet qui consiste à administrer à ce sujet un ou plusieurs réovirus et un de plusieurs agents qui modulent l'expression ou l'activité de cytokines pro-inflammatoires. Par exemple, les agents peuvent inhiber l'expression ou l'activité de cytokines pro-inflammatoires.
PCT/CA2009/000721 2008-05-27 2009-05-27 Suppression de production de cytokines pro-inflammatoires pendant une thérapie par réovirus oncolytique WO2009143611A1 (fr)

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CN2009801193973A CN102065873A (zh) 2008-05-27 2009-05-27 在溶瘤呼肠孤病毒治疗中消除促炎细胞因子的产生
CA2723587A CA2723587C (fr) 2008-05-27 2009-05-27 Suppression de production de cytokines pro-inflammatoires pendant une therapie par reovirus oncolytique
AU2009253683A AU2009253683B2 (en) 2008-05-27 2009-05-27 Abrogating proinflammatory cytokine production during oncolytic reovirus therapy
JP2011510788A JP2011520994A (ja) 2008-05-27 2009-05-27 腫瘍崩解性レオウイルス療法中の炎症性サイトカイン産生の排除
EP09753372A EP2296679A4 (fr) 2008-05-27 2009-05-27 Suppression de production de cytokines pro-inflammatoires pendant une thérapie par réovirus oncolytique
US12/994,114 US8470312B2 (en) 2008-05-27 2009-05-27 Abrogating proinflammatory cytokine production during oncolytic reovirus therapy
MX2010012857A MX2010012857A (es) 2008-05-27 2009-05-27 Supresion de produccion de citoquina proinflamatoria durante la terapia de reovirus oncolitico.
IL208380A IL208380A (en) 2008-05-27 2010-10-03 Use of a virus and platinum compound to manufacture a drug for the treatment of proliferative disorder and pharmaceuticals
ZA2010/08017A ZA201008017B (en) 2008-05-27 2010-11-09 Abrogating proinflammatory cytokine production during oncolytic reovirus therapy
US13/898,771 US20130243732A1 (en) 2008-05-27 2013-05-21 Abrogating proinflammatory cytokine production during oncolytic reovirus therapy

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